Nephritic Syndrome Flashcards

1
Q

What is nephritic syndrome

A

Syndrome fitting the clinical picture of inflammation within the kidney

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2
Q

Defining features of nephritic syndrome

A

Haeamaturia - reflects inflammation of the kidney

Oliguria - due to reduced GFR

Proteinuria - less than 3g/ 24hrs

Hypertension - due to fluid overload

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3
Q

Systemic causes of nephritic syndrome

A

SLE
Post strep GN
Iga nephropathy
good pastures

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4
Q

GS diagnostic test for nephritic syndrome?

A

kidney biopsy

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5
Q

Other investigations for nephritic syndrome

A

Urinalysis - shows haematuria in nephritic syndrome
Bloods- elevated ESR and CRP in inflammation ; may be anaemia

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6
Q

What is an ESR test and what does it do

A

Erythrocyte sedimentantion rate

Test measure how fast/ slow RBC will sink / settle

Inflammation causes RBC to clump together which are heavier to sink faster

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7
Q

What does a CRP test do and show

A

C reactive protein is made in the liver

more is released in response to inflammation

can only diagnose inflammation not the cause of it

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8
Q

Management of nephritic syndrome

A

Blood pressure control- ACE/ ARB, reduces proteinuria and preserves renal function

Corticosteroids- reduce inflammation causing damage to the kidney

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9
Q

What is Iga nephropathy

A

Defined by the presence of mesangial Iga immune deposits

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10
Q

Explain the pathophysiology of Iga nepropathy

A

immune complexes are formed –
become trapped in glomeruli– deposit in mesangial area which normally offers structural support to glomeruli

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11
Q

Key diagnostic factor of Iga nephropathy

A

Haematuria - blood in urine

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12
Q

How are ace inhibitors effective in iga nephropathy

A
  • decrease the pressure of blood entering kidneys
  • decrease inflammatory damage
  • slow progression of the disease
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13
Q

What would immunofluorescence microscopy show for iga neprhopathy

A

Iga complex deposition

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14
Q

What is post streptococcal glomerulonephritis

A

Where the kidneys glomeruli become inflamed after an infection by streptococcal bacteria

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15
Q

When would PSGN usually present

A

1-2 weeks after pharyngitis from group a b haemolytic strep

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16
Q

Diagnosis of PSGN would show ?

A

Light microscope- hypercellular glomeruli

Immunofluorescence shows - starry sky appearance and igg and igm deposits

electron microscope- subendothelial immune complex deposition

17
Q

treatment for PSGN

A
  • Furosemide: for initial treatment of hypertension
  • Antibiotics
18
Q

Pathophsyiology for PSGN

A
  • Group a streptococci carry M protein virulence factor which initiates a type 3 hypersensitivity reaction
  • the immune complex depositions travel to the glomerular basement membrane and deposit
  • the deposit initiates an inflammatory reaction which invovles activation of C3 complement,
19
Q

clinical manifestations for psgn

A

Haematuria
signs of recent infection

20
Q

What occurs in good pastures syndrome

A

ANTI GBM antibodies attack the glomerulus and pulmonary basement membrane

This causes glomerulonephritis and pulmonary haemorrhage

21
Q

Typical presentation of good pastures syndrome

A

acute kidney failure and haemoptysis (coughing of blood)

22
Q

What is the most common cause of primary glomerulonephritis

A

iga nephropathy

23
Q

What is the most common type of glomerulonephritis overall

A

membranous glomerunephritis

24
Q

Key causes for both nephrotic and nephritic syndrome

A

diffuse proliferative GN
membranoproliferative GN

25
What is IgA nephropathy?
Deposition of IgA into mesangium of kidney - causes inflammation and damage Presents asymptomatically with microscopic haematuria Diagnose by biopsy Give fish oil and steroids for persisten proteinuria after 3-6 months
26
What is goodpastures disease
Goodpasture syndrome is an autoimmune disease that primarily affects the lungs and the kidneys. Also known as anti-GBM disease and is a rare small-vessel vasculitis.
27
What is post strep glomerulonephritis (cause of glomerulonephritis)
Deposition of strep antigens post infection Presents with haematuria and acute nephritis Diagnose with eviden of strep infection Antibiotics and supportive care
28
Henoch choenlein purpura (Cause of glomerulonephritis)
Small vessel vasculitis Affects kidneys and joints due to IgA deposition
29
Triad of symptoms for nephrotic syndrome
Hypoalbuniaemia (loss of albumin in urine) Proteinuria (>3g/24hr) Oedema - loss of albumin therefore loss of oncotic pressure
30
Causes of nephrotic syndrome
Minimal change disease Focal segmental glomerulosclerosis Membranous nephropathy c